Gid Project Manager
Il y a 7 mois
**GID Project Manager**
The success of a company depends on the passionate people we partner with.
Together, let's share our talents.
As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing, producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet.
We are committed to ensuring the highest possible level of care and well-being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife.
Indeed, Our “Together, Beyond Animal Health” vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach.
As part of our “Diversity, Equity and Inclusion” policy, Ceva Animal Heath is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team.
**Your missions**:
For our industrial site in Libourne (33), we are looking for an industrial development project manager.
YOUR MISSIONS
Within the GID - Global Industrial Development - department and under the supervision of the department manager, the incumbent: I/ Will ensure, within the framework of strategic industrial projects, in particular new products and product transfers, the industrial transposition from the development phase to the commercial phase:
- By participating in the definition of the industrialization strategy
- By participating in the choice of processes during pharmaceutical development (Quality by Design)
- By coordinating activities with other R&D and industrial departments,
- By writing protocols and reports for process optimization and validation,
- By monitoring the production of batches according to Good Manufacturing Practices, and analyzing the results (statistical analyses), - By making available to manufacturers, marketing and operations, products that meet their requirements and the requirements of the market, - Respecting the cost, the study deadlines and the conformity of the products with the specifications
- By integrating technical and regulatory developments II/
Will participate, as part of the site's technical support activities:
- meetings to validate changes in supplier or process, - trouble shooting meetings of the production department during investigations linked to problems linked to manufacturing processes
- by developing the various galenic or industrial tests to be implemented and by leading risk analysis sessions (FMEA).
Will participate in the operation of the service: writing procedures, participation in self-inspections, documentary archiving, service meetings.
**Your profile**:
- Trained as an engineer and/or pharmacist, you have at least 3 years of experience in a pharmaceutical industrial environment.
- You have significant experience in project management: coordination of multidisciplinary teams and facilitation of project meetings.
- Preferable knowledge of the manufacturing processes for injectable forms, environmental constraints and the associated regulatory context
- Notions of Quality by Design, use of Minitab type software, would be a plus
- You have an aptitude for teamwork, a capacity for analysis and synthesis, are rigorous and capable of managing different projects at different stages of development.
- You have the ability to interact in writing and orally in an English-speaking environment.
- Very punctual 3x8 schedules - Occasional trips possible in France or abroad
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